Services
Choose from a large library of standard modules for all main purposes and therapeutic areas. We have built in our experiences from many years and transformed them into a world-class CRF library that fully supports industry standards, such as those of the Clinical Data Interchange Standards Consortium (CDISC).
Accovion can design your CRF for optimal collection of data in accordance with the study protocol, whether you want to use paper or eCRFs, including the patient’s diary.
Quality data and “investigator friendly”
Quality questionnaires will generate quality data. Our experience prevents collecting misleading information. We ask only relevant and important questions, specific enough for compliance with the protocol and the underlying indication and clear enough to be self-explanatory. Investigators like our CRFs because they speak the medical language, don’t ask repetitive questions and are easy to complete.
Carole Martini
Director Clinical Data Management
+49 6196 7709-433
